Variant report
| Variant | rs6930567 |
|---|---|
| Chromosome Location | chr6:54559478-54559479 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr6:54558970..54566519-chr6:54708534..54713743,16 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000168143 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:24)
| rs_ID | r2[population] |
|---|---|
| rs10484987 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs10484990 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
| rs10484992 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs10948833 | 1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes] |
| rs12192965 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
| rs12194292 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
| rs12194478 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
| rs12198783 | 0.89[ASN][1000 genomes] |
| rs12205849 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
| rs12206020 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs12208354 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs12209646 | 0.89[ASN][1000 genomes] |
| rs12211249 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs12213260 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs66999431 | 0.93[EUR][1000 genomes] |
| rs6906762 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs6927382 | 0.89[ASN][1000 genomes] |
| rs6934575 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
| rs7743287 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs7773204 | 0.89[ASN][1000 genomes] |
| rs7775692 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
| rs925056 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
| rs9474982 | 0.89[ASN][1000 genomes] |
| rs9474983 | 0.89[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv885900 | chr6:54517968-54852462 | Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
